Variant #0000480271 (NC_000019.9:g.13002736del, NM_000159.3:c.219del (GCDH))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method ACMG
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.13002736del
DNA change (hg38) g.12891922del
Published as -
ISCN -
DB-ID GCDH_000066 See all 10 reported entries
Variant remarks ACMG/ACGS: PS4_Moderate, PM3_Strong, PP4, PVS1, PM2_Supporting (December 2023)
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Isabelle Rinke
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-05-22 09:22:27 +02:00 (CEST)
Date last edited 2024-11-11 14:57:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCDH NM_000159.3 +/+ 4 c.219del r.(?) p.(Tyr74Thrfs*68)


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